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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880349Generated: October 25, 2026

Ethylenediamine → Brimonidine

https://huagongshe.com/reaction/880349

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylenediamineHCID 3301—
Reactant5-Bromo-6-isothiocyanatoquinoxalineHCID 4460274—
SolventBenzeneHCID 241—
ProductBrimonidineHCID 2435—

Reaction Steps

The 5-bromo-6-isothiocyanato-quinoxaline (3.5 g.) is directly dissolved in benzene (400 ml) and added dropwise to a well-stirred solution of ethylene diamine (15 g.) in benzene (50 ml). During a period of about two hours, an oil separates as a lower layer. The upper benzene layer is poured off and the oil is washed with diethyl ether and then dissolved in methanol (500 ml). The methanolic solution is refluxed until hydrogen sulfide evolution ceases. The methanolic solution is concentrated in vacuo to a volume of approximately 100 ml upon which a yellow solid precipitates. The precipitate is collected by filtration and recrystallized from methanol to afford of (5-Bromo-quinoxalin-6-yl)-(4,5-dihydro-1H-imidazol-2-yl)-amine: m.p. 250-251 C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993571B2
Source datasetuspto-grants-2015_03
ORD IDord-b3bea7d9a6b04d1eb504156ae990065f
Source noteuspto-grants-2015_03